Aydoğan Cemil, El Rassi Ziad
Department of Chemistry, Oklahoma State University, Stillwater OK, USA.
Department of Chemistry, Oklahoma State University, Stillwater OK, USA.
J Chromatogr A. 2016 May 6;1445:62-7. doi: 10.1016/j.chroma.2016.03.083. Epub 2016 Apr 1.
This study is concerned with the incorporation of surface modified fumed silica nanoparticles (FSNPs) into polymethacrylate based monolithic columns for use in reversed phase chromatography (RPC) of small solutes and proteins. First, FSNPs were modified with 3-(trimethoxysilyl)propylmethacrylate (TMSPM) to yield the "hybrid" methacryloyl fumed silica nanoparticle (MFSNP) monomer. The resulting MFSNP was then mixed with glyceryl monomethacrylate (GMM) and ethylene dimethacrylate (EDMA) in a binary porogenic solvent composed of cyclohexanol and dodecanol, and the in situ copolymerization of MFSNP, GMM and EDMA was performed in a stainless steel column of 4.6 mm i.d. The silanol groups of the hybrid monolith thus obtained were grafted with octadecyl ligands by perfusing the hybrid monolithic column with a solution of 4% w/v of dimethyloctadecylchlorosilane (DODCS) in toluene while the column was maintained at 110°C for 6h (in a heated HPLC oven). One of the originalities of this study was to demonstrate MFSNP as a novel derivatized "hybrid monomer" in making RPC monolithic columns with surface bound octadecyl ligands. In this respect, the RPC behavior of the monolithic column with "covalently" incorporated FNSPs having surface grafted octadecyl ligands was evaluated with alkylbenzenes, aniline derivatives and phenolic compounds. The results showed that the hybrid poly(GMA-EDMA-MFSNP) having surface bound octadecyl ligands exhibited hydrophobic interactions under reversed phase elution conditions. Furthermore, six standard proteins were baseline separated on the column using a 10min linear gradient elution at increasing ACN concentration in the mobile phase at a flow rate of 1.0mL/min using a 10 cm×4.6mm i.d. column. The relative standard deviations (RSDs) for the retention times of the tested solutes were lower than 2.1% and 2.4% under isocratic elution and gradient elution conditions, respectively.
本研究关注将表面改性的气相二氧化硅纳米颗粒(FSNPs)掺入基于聚甲基丙烯酸酯的整体柱中,用于小溶质和蛋白质的反相色谱(RPC)。首先,用甲基丙烯酸3-(三甲氧基硅基)丙酯(TMSPM)对FSNPs进行改性,得到“杂化”甲基丙烯酰基气相二氧化硅纳米颗粒(MFSNP)单体。然后将所得的MFSNP与甲基丙烯酸甘油酯(GMM)和二甲基丙烯酸乙二酯(EDMA)在由环己醇和十二烷醇组成的二元致孔溶剂中混合,并在内径为4.6 mm的不锈钢柱中进行MFSNP、GMM和EDMA的原位共聚。通过在110°C下将4% w/v的二甲基十八烷基氯硅烷(DODCS)甲苯溶液灌注到杂化整体柱中6小时(在加热的高效液相色谱柱箱中),将由此获得的杂化整体柱的硅醇基团用十八烷基配体进行接枝。本研究的一个创新之处在于证明MFSNP作为一种新型衍生化的“杂化单体”用于制备具有表面键合十八烷基配体的RPC整体柱。在这方面,用烷基苯、苯胺衍生物和酚类化合物评估了具有表面接枝十八烷基配体的“共价”掺入FNSPs的整体柱的RPC行为。结果表明,具有表面键合十八烷基配体的杂化聚(GMA-EDMA-MFSNP)在反相洗脱条件下表现出疏水相互作用。此外,使用内径为10 cm×4.6 mm的柱,在流动相ACN浓度增加的情况下,以1.0 mL/min的流速进行10分钟线性梯度洗脱,六种标准蛋白质在该柱上实现了基线分离。在等度洗脱和梯度洗脱条件下,测试溶质保留时间的相对标准偏差(RSD)分别低于2.1%和2.4%。